Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record. - Test2 - elhamkhani - TriplyDB

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.

Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.

http://www.wikidata.org/entity/Q33773017

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Chapter 11: Genome-wide association studies Sequencing and analysis of a South Asian-Indian personal genome Identification of genomic predictors of atrioventricular conduction: using electronic medical records as a tool for genome science Validating drug repurposing signals using electronic health records: a case study of metformin associated with reduced cancer mortality Translational bioinformatics: linking the molecular world to the clinical world Leveraging the electronic health record to implement genomic medicine Identifiability in biobanks: models, measures, and mitigation strategies Mining electronic health records: towards better research applications and clinical care Secondary consent to biospecimen use in a prostate cancer biorepository Meta-analysis of shared genetic architecture across ten pediatric autoimmune diseases Surveying Recent Themes in Translational Bioinformatics: Big Data in EHRs, Omics for Drugs, and Personal Genomics Deciphering Signaling Pathway Networks to Understand the Molecular Mechanisms of Metformin Action Extracting research-quality phenotypes from electronic health records to support precision medicine Self-reported race/ethnicity in the age of genomic research: its potential impact on understanding health disparities Technical challenges for big data in biomedicine and health: data sources, infrastructure, and analytics Secondary use of clinical data: the Vanderbilt approach Validation and enhancement of a computable medication indication resource (MEDI) using a large practice-based dataset The Electronic Medical Records and Genomics (eMERGE) Network: past, present, and future Development and evaluation of an ensemble resource linking medications to their indications Efficient replication of over 180 genetic associations with self-reported medical data Anonymization of administrative billing codes with repeated diagnoses through censoring Biobanking in pediatrics: the human nonsubjects approach Using Electronic Patient Records to Discover Disease Correlations and Stratify Patient Cohorts A common 5'-UTR variant in MATE2-K is associated with poor response to metformin.Using previously genotyped controls in genome-wide association studies (GWAS): application to the Stroke Genetics Network (SiGN)Type 2 diabetes risk forecasting from EMR data using machine learning.Computational phenotype discovery using unsupervised feature learning over noisy, sparse, and irregular clinical data Applying active learning to high-throughput phenotyping algorithms for electronic health records data The Mid-South clinical Data Research Network.Modular design, application architecture, and usage of a self-service model for enterprise data delivery: the Duke Enterprise Data Unified Content Explorer (DEDUCE)Extraction of echocardiographic data from the electronic medical record is a rapid and efficient method for study of cardiac structure and function.Enhancing uterine fibroid research through utilization of biorepositories linked to electronic medical record data.Identification of Nonresponse to Treatment Using Narrative Data in an Electronic Health Record Inflammatory Bowel Disease Cohort.Knowledge-driven multi-locus analysis reveals gene-gene interactions influencing HDL cholesterol level in two independent EMR-linked biobanks.Validity of cluster headache diagnoses in an electronic health record data repository.The impact of common dopamine D2 receptor gene polymorphisms on D2/3 receptor availability: C957T as a key determinant in putamen and ventral striatum.Genetic-based prediction of disease traits: prediction is very difficult, especially about the future Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank.Data from clinical notes: a perspective on the tension between structure and flexible documentation.Phenome-Wide Association Studies as a Tool to Advance Precision Medicine.

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Robust replication of genotype-phenotype associations across multiple diseases in an electronic medical record.

http://www.wikidata.org/entity/Q33773017

description

2010 nî lūn-bûn

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2010 թուականի Ապրիլին հրատարակուած գիտական յօդուած

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2010 թվականի ապրիլին հրատարակված գիտական հոդված

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2010年の論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年論文

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2010年论文

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Robust replication of genotype ...... an electronic medical record.

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Robust replication of genotype ...... an electronic medical record.

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J.AJHG.2010.03.003

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American Journal of Human Genetics

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Robust replication of genotype ...... an electronic medical record.

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Andrea H Ramirez

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Dan M Roden

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Daniel R Masys

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Jeffrey R Balser

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Jill M Pulley

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Joshua C Denny

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Justin B Weiner

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Kristin Brown-Gentry

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Melissa A Basford

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P2860

Genome-wide association defines more than 30 distinct susceptibility loci for Crohn's disease

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

Collaborative genome-wide association studies of diverse diseases: programs of the NHGRI's office of population genomics

A haplotype map of the human genome

Replication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetes

Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels

Sequence variants in the autophagy gene IRGM and multiple other replicating loci contribute to Crohn's disease susceptibility

Risk alleles for multiple sclerosis identified by a genomewide study

"Understanding" medical school curriculum content using KnowledgeMap

Integration of genomic data in Electronic Health Records--opportunities and dilemmas.

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560-572

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10.1016/J.AJHG.2010.03.003

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Marylyn D. Ritchie

Jonathan L Haines

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2010-04-01T00:00:00Z

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42974151

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